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Transfers multiple

Enantioselective Addition of Organometallic Reagents to Carbonyl Compounds Chirality Transfer, Multiplication, and Amplification 255... [Pg.199]

A wide variety of methodologies and reagents are currently employed to introduce different molecules into eukaryotic cells. The incorporation of DNA can be achieved by two different mechanisms infection or transfection. The first consists of a biological process mediated by a virus (the viral infection of cells is mediated by receptors), while the second makes use of physical or biochemical methods to incorporate the DNA into the cell. Although the virus-mediated methods are more efficient, they are more laborious and time-consuming compared with transfection. Additionally, the nature of the infection process requires the presence of virus-specific receptors in the host cell to allow viral penetration, which restricts the spectrum of possible host cells. Another limitation of viral infection as a method for DNA transfer is that, unlike plasmid transfection, it is not possible to simultaneously transfer multiple recombinant viruses into the cell (Wurm and Bernard, 1999). [Pg.58]

R. Noyori, M. Kitamura, Enantioselective Addition of Oiganometallic Reagents to Ccarbonyl Compounds Chirality Transfer, Multiplication and Amplification, Angew. Chem. Int. Ed. Engl. 1991, 30, 49. [Pg.453]

To understand the pulse sequence, we will try to get an overview of what is happening and then look at some simplified product operator analysis. Consider first the CH case in the DEPT-90 experiment. Ignoring the 180° pulses, the DEPT-90 sequence can be viewed as an INEPT sequence in which the coherence transfer is split up into two steps (Fig. 7.41) the two 90° pulses are no longer simultaneous and between them we have an intermediate state in coherence transfer multiple-quantum coherence (ZQC and DQC). [Pg.283]

In addition, for value transfer, multiple weight-corrected dilutions of the reference (e.g., CRM 470) and the target material should be assayed in multiple runs, with the dilutions of each material calculated to be within the same section of the assay range. If possible, for optimal results, one material should be used as the cafibrator and the other as the test sample to avoid the introduction of a third material and increased imprecision. ... [Pg.583]

Noyori R, Kitamura M (1991) Enantioselective addition of organometallic reagents to carbonyl-compounds - chirality transfer, multiplication, and amplification. Angew Chem Int Ed 30 49-69... [Pg.223]

The results presented are encouraging to continuing efforts to prepare catalysts with the capacity to transfer multiple electrons at the same energy. Numerous analogs of the successful CoP(pyRuNH3)5)4 catalyst can be envisioned which could behave similarly, or even better, as multiple-electron transfer agents. [Pg.389]

Noyori, R. and Kitamura, M. (1 1) Enantioselective addition of organometallic reagents to cartenyl compounds chirality, transfer, multiplication and amplification, Aitgew. Chem. Int. Ed. Engl 30,49. ... [Pg.24]

Of the Group 8 homobimetallic complexes, those of diruthenium are the most numerous, perhaps because of their stability. Diruthenium complexes have many interesting electronic and redox properties. They can have multiple bonds, and they can be low or intermediate spin. Moreover, the spin states can be explained by the application of simple ligand field theory. Diruthenium complexes have been isolated in several redox states. Typically, oxidation state changes result in minimal reorganization of the diruthenium core, and hence, many of these complexes can transfer multiple electrons readily, albeit one at a time. [Pg.237]

Mass transfer processes are complicated, usually involving turbulent flow, heat transfer, multiple phases, chemical reactions, unsteady operation, as well as the influences from internal construction of the equipment and many other factors. To study such complicated system, we propose a novel scientific computing framework in which all the relevant equations on mass transfer, fluid-dynamics, heat transfer, chemical reactions, and all other influencing factors are involved and solved numerically. This is the main task and research methodology of computational mass transfer (CMT). [Pg.342]


See other pages where Transfers multiple is mentioned: [Pg.274]    [Pg.122]    [Pg.517]    [Pg.1252]    [Pg.331]    [Pg.192]    [Pg.359]    [Pg.354]    [Pg.46]    [Pg.76]    [Pg.274]    [Pg.254]    [Pg.865]    [Pg.102]    [Pg.1146]    [Pg.31]    [Pg.255]    [Pg.287]    [Pg.282]    [Pg.285]    [Pg.12]    [Pg.992]    [Pg.431]    [Pg.6]   
See also in sourсe #XX -- [ Pg.231 ]

See also in sourсe #XX -- [ Pg.231 ]




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Current multiple-electron transfers

Electrode potential multiple electron transfer

Electrode processes involving multiple electron transfer

Electron storage and transfer in organic redox systems with multiple

Electron storage and transfer in organic redox systems with multiple electrophores

Electrons transferring multiple

Hydride transfer reactions, multiple reaction

Multiple Hydrogen Transfer

Multiple Hydrogen Transfer in H-bonds of Medium Strength

Multiple Hydrogen Transfers in Enzyme Action

Multiple Phases-Mass Transfer

Multiple Proton Transfer From Stepwise to Concerted

Multiple electron transfer

Multiple electron-transfer reactions

Multiple magnetization transfers

Multiple magnetization transfers spin-diffusion)

Multiple quantum coherence transfer

Multiple quantum coherence transfer HMQC)

Multiple quantum transfer echo

Multiple-Electron Transfer Processes

Multiple-Electron Transfers Adaptive Spatial Grids

Multiple-pulse sequence transfer efficiency

Proton transfer multiple

Radiative transfer multiple scattering

Redox systems, organic, with multiple electrophores, electron storage and transfer

Redox systems, organic, with multiple transfer

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